Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933436I01Rik |
T |
A |
X: 66,964,308 (GRCm39) |
I184L |
probably benign |
Het |
A2ml1 |
A |
T |
6: 128,529,271 (GRCm39) |
M957K |
probably benign |
Het |
Adam7 |
C |
A |
14: 68,742,610 (GRCm39) |
V668F |
probably benign |
Het |
Adcy7 |
T |
G |
8: 89,038,902 (GRCm39) |
L306R |
probably damaging |
Het |
Akt3 |
A |
G |
1: 176,930,551 (GRCm39) |
S136P |
possibly damaging |
Het |
Alox12e |
G |
A |
11: 70,206,828 (GRCm39) |
R620W |
probably damaging |
Het |
Amy2a1 |
T |
C |
3: 113,324,217 (GRCm39) |
I108V |
probably benign |
Het |
Ano7 |
T |
C |
1: 93,318,035 (GRCm39) |
V249A |
probably benign |
Het |
Aox1 |
T |
C |
1: 58,098,351 (GRCm39) |
|
probably null |
Het |
Asah2 |
A |
T |
19: 32,002,274 (GRCm39) |
V290E |
probably damaging |
Het |
Ascc2 |
A |
T |
11: 4,631,496 (GRCm39) |
M646L |
probably benign |
Het |
Atxn2l |
T |
A |
7: 126,095,038 (GRCm39) |
K421N |
probably damaging |
Het |
Cars2 |
T |
C |
8: 11,597,747 (GRCm39) |
I110V |
probably damaging |
Het |
Ccdc74a |
A |
G |
16: 17,467,890 (GRCm39) |
N249S |
probably benign |
Het |
Cenpe |
T |
C |
3: 134,928,082 (GRCm39) |
|
probably benign |
Het |
Clptm1l |
C |
T |
13: 73,755,842 (GRCm39) |
Q153* |
probably null |
Het |
Cnep1r1 |
G |
T |
8: 88,845,445 (GRCm39) |
|
probably benign |
Het |
Cyp2d37-ps |
C |
T |
15: 82,574,289 (GRCm39) |
|
noncoding transcript |
Het |
Cyp3a25 |
A |
G |
5: 145,923,779 (GRCm39) |
|
probably benign |
Het |
Dis3l |
G |
T |
9: 64,246,855 (GRCm39) |
Q67K |
probably benign |
Het |
Dnah1 |
A |
G |
14: 30,993,086 (GRCm39) |
V2936A |
probably damaging |
Het |
Dnah5 |
C |
T |
15: 28,366,416 (GRCm39) |
R2710C |
probably damaging |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
Dvl3 |
G |
A |
16: 20,345,101 (GRCm39) |
S361N |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Eif2ak3 |
T |
C |
6: 70,881,181 (GRCm39) |
V1085A |
probably benign |
Het |
Eif3b |
T |
C |
5: 140,412,208 (GRCm39) |
Y226H |
probably damaging |
Het |
Endov |
T |
C |
11: 119,390,408 (GRCm39) |
F12S |
probably damaging |
Het |
Ercc1 |
A |
G |
7: 19,088,295 (GRCm39) |
*37W |
probably null |
Het |
Evi2a |
G |
A |
11: 79,418,593 (GRCm39) |
Q6* |
probably null |
Het |
Faah |
C |
T |
4: 115,855,770 (GRCm39) |
V552M |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,477,369 (GRCm39) |
N2138K |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,479,741 (GRCm39) |
V2929E |
probably damaging |
Het |
Gm2959 |
A |
G |
14: 42,235,658 (GRCm39) |
|
noncoding transcript |
Het |
Gm6327 |
A |
T |
16: 12,578,979 (GRCm39) |
|
noncoding transcript |
Het |
Gm9912 |
T |
C |
3: 148,890,795 (GRCm39) |
T113A |
unknown |
Het |
Gtf2f2 |
A |
G |
14: 76,155,136 (GRCm39) |
S142P |
possibly damaging |
Het |
Hspg2 |
A |
T |
4: 137,286,678 (GRCm39) |
T3666S |
possibly damaging |
Het |
Htt |
C |
T |
5: 34,983,326 (GRCm39) |
T975I |
probably benign |
Het |
Il2rg |
A |
G |
X: 100,311,416 (GRCm39) |
L57P |
possibly damaging |
Het |
Iqgap1 |
G |
A |
7: 80,373,727 (GRCm39) |
Q1421* |
probably null |
Het |
Itga3 |
T |
A |
11: 94,944,902 (GRCm39) |
Q802L |
possibly damaging |
Het |
Lonp2 |
A |
G |
8: 87,392,403 (GRCm39) |
T490A |
probably damaging |
Het |
Lztr1 |
T |
C |
16: 17,327,534 (GRCm39) |
V79A |
probably damaging |
Het |
Mast4 |
C |
T |
13: 102,895,601 (GRCm39) |
E736K |
probably benign |
Het |
Mpp4 |
G |
A |
1: 59,182,941 (GRCm39) |
P322L |
possibly damaging |
Het |
Mrto4 |
T |
C |
4: 139,076,334 (GRCm39) |
K86E |
probably benign |
Het |
Myof |
A |
G |
19: 37,904,194 (GRCm39) |
V2A |
possibly damaging |
Het |
Naf1 |
A |
G |
8: 67,340,432 (GRCm39) |
D414G |
probably damaging |
Het |
Nbea |
A |
G |
3: 55,993,578 (GRCm39) |
|
probably benign |
Het |
Nebl |
A |
T |
2: 17,401,932 (GRCm39) |
M427K |
probably benign |
Het |
Ngdn |
T |
C |
14: 55,259,564 (GRCm39) |
V205A |
possibly damaging |
Het |
Nup133 |
C |
A |
8: 124,641,314 (GRCm39) |
D869Y |
probably damaging |
Het |
Oas1g |
T |
C |
5: 121,023,946 (GRCm39) |
E121G |
probably damaging |
Het |
Or10j3b |
T |
C |
1: 173,043,277 (GRCm39) |
F20L |
probably benign |
Het |
Or2ab1 |
A |
G |
11: 58,488,396 (GRCm39) |
N58S |
probably damaging |
Het |
Or2w3 |
G |
T |
11: 58,556,808 (GRCm39) |
C141F |
probably damaging |
Het |
Or5m9 |
A |
G |
2: 85,877,299 (GRCm39) |
T158A |
probably damaging |
Het |
Or6c205 |
T |
A |
10: 129,087,001 (GRCm39) |
Y199* |
probably null |
Het |
Park7 |
T |
C |
4: 150,989,732 (GRCm39) |
N76S |
probably benign |
Het |
Pcdh8 |
A |
T |
14: 80,005,651 (GRCm39) |
S912R |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,271,559 (GRCm39) |
I2998T |
probably damaging |
Het |
Plxnb3 |
T |
A |
X: 72,815,357 (GRCm39) |
Y1845* |
probably null |
Het |
Ppard |
A |
G |
17: 28,518,663 (GRCm39) |
H388R |
probably damaging |
Het |
Psma1 |
A |
G |
7: 113,869,001 (GRCm39) |
S142P |
possibly damaging |
Het |
Pth2r |
T |
C |
1: 65,382,721 (GRCm39) |
I158T |
probably damaging |
Het |
Rbl2 |
C |
A |
8: 91,833,367 (GRCm39) |
P714Q |
probably damaging |
Het |
Rexo2 |
A |
T |
9: 48,385,813 (GRCm39) |
S104T |
possibly damaging |
Het |
Sema5a |
T |
C |
15: 32,609,363 (GRCm39) |
|
probably benign |
Het |
Spmip10 |
C |
T |
18: 56,721,535 (GRCm39) |
Q25* |
probably null |
Het |
Sun2 |
A |
G |
15: 79,622,852 (GRCm39) |
L109P |
probably damaging |
Het |
Tdg |
A |
G |
10: 82,477,368 (GRCm39) |
T116A |
probably benign |
Het |
Terb1 |
A |
T |
8: 105,195,380 (GRCm39) |
M587K |
possibly damaging |
Het |
Tmcc1 |
C |
T |
6: 116,020,019 (GRCm39) |
V118M |
probably benign |
Het |
Tnfsf11 |
T |
A |
14: 78,516,362 (GRCm39) |
N202I |
probably damaging |
Het |
Togaram2 |
T |
C |
17: 72,023,360 (GRCm39) |
S759P |
probably benign |
Het |
Ttc7b |
G |
A |
12: 100,291,948 (GRCm39) |
A208V |
probably damaging |
Het |
Tti2 |
T |
C |
8: 31,644,338 (GRCm39) |
|
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,905,118 (GRCm39) |
|
probably null |
Het |
Zfyve26 |
T |
C |
12: 79,330,806 (GRCm39) |
|
probably null |
Het |
Zfyve28 |
T |
C |
5: 34,391,681 (GRCm39) |
M157V |
probably null |
Het |
Zgrf1 |
T |
C |
3: 127,406,999 (GRCm39) |
C1589R |
probably damaging |
Het |
|
Other mutations in Nav3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00095:Nav3
|
APN |
10 |
109,677,594 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00425:Nav3
|
APN |
10 |
109,539,368 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00465:Nav3
|
APN |
10 |
109,688,607 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00531:Nav3
|
APN |
10 |
109,539,171 (GRCm39) |
missense |
probably null |
0.99 |
IGL00575:Nav3
|
APN |
10 |
109,600,626 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00770:Nav3
|
APN |
10 |
109,652,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00774:Nav3
|
APN |
10 |
109,652,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00858:Nav3
|
APN |
10 |
109,578,493 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00935:Nav3
|
APN |
10 |
109,541,527 (GRCm39) |
missense |
probably benign |
|
IGL01638:Nav3
|
APN |
10 |
109,688,724 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01662:Nav3
|
APN |
10 |
109,605,119 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01670:Nav3
|
APN |
10 |
109,550,102 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01885:Nav3
|
APN |
10 |
109,578,521 (GRCm39) |
nonsense |
probably null |
|
IGL01979:Nav3
|
APN |
10 |
109,540,790 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02121:Nav3
|
APN |
10 |
109,594,897 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02210:Nav3
|
APN |
10 |
109,602,851 (GRCm39) |
missense |
probably benign |
|
IGL02523:Nav3
|
APN |
10 |
109,605,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02573:Nav3
|
APN |
10 |
109,702,835 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02633:Nav3
|
APN |
10 |
109,527,997 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02810:Nav3
|
APN |
10 |
109,652,135 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02964:Nav3
|
APN |
10 |
109,572,814 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03015:Nav3
|
APN |
10 |
109,554,158 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03288:Nav3
|
APN |
10 |
109,594,878 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03310:Nav3
|
APN |
10 |
109,660,433 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4377001:Nav3
|
UTSW |
10 |
109,552,466 (GRCm39) |
missense |
probably damaging |
0.99 |
R0010:Nav3
|
UTSW |
10 |
109,659,087 (GRCm39) |
splice site |
probably benign |
|
R0043:Nav3
|
UTSW |
10 |
109,603,379 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0053:Nav3
|
UTSW |
10 |
109,602,778 (GRCm39) |
splice site |
probably benign |
|
R0053:Nav3
|
UTSW |
10 |
109,602,778 (GRCm39) |
splice site |
probably benign |
|
R0077:Nav3
|
UTSW |
10 |
109,552,503 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0219:Nav3
|
UTSW |
10 |
109,702,791 (GRCm39) |
critical splice donor site |
probably null |
|
R0310:Nav3
|
UTSW |
10 |
109,602,989 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0380:Nav3
|
UTSW |
10 |
109,594,740 (GRCm39) |
splice site |
probably benign |
|
R0403:Nav3
|
UTSW |
10 |
109,602,964 (GRCm39) |
missense |
probably damaging |
0.98 |
R0480:Nav3
|
UTSW |
10 |
109,689,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:Nav3
|
UTSW |
10 |
109,659,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R0637:Nav3
|
UTSW |
10 |
109,606,058 (GRCm39) |
missense |
probably benign |
0.25 |
R0847:Nav3
|
UTSW |
10 |
109,739,718 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0988:Nav3
|
UTSW |
10 |
109,552,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R1272:Nav3
|
UTSW |
10 |
109,572,860 (GRCm39) |
missense |
probably damaging |
0.98 |
R1295:Nav3
|
UTSW |
10 |
109,527,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R1405:Nav3
|
UTSW |
10 |
109,606,194 (GRCm39) |
splice site |
probably benign |
|
R1406:Nav3
|
UTSW |
10 |
109,719,495 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1406:Nav3
|
UTSW |
10 |
109,719,495 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1420:Nav3
|
UTSW |
10 |
109,659,115 (GRCm39) |
missense |
probably benign |
0.02 |
R1449:Nav3
|
UTSW |
10 |
109,689,372 (GRCm39) |
missense |
probably benign |
0.13 |
R1458:Nav3
|
UTSW |
10 |
109,555,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Nav3
|
UTSW |
10 |
109,596,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Nav3
|
UTSW |
10 |
109,596,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1472:Nav3
|
UTSW |
10 |
109,563,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R1537:Nav3
|
UTSW |
10 |
109,702,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R1539:Nav3
|
UTSW |
10 |
109,603,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R1581:Nav3
|
UTSW |
10 |
109,659,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R1586:Nav3
|
UTSW |
10 |
109,689,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Nav3
|
UTSW |
10 |
109,688,984 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1725:Nav3
|
UTSW |
10 |
109,659,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1742:Nav3
|
UTSW |
10 |
109,605,074 (GRCm39) |
missense |
probably benign |
|
R1793:Nav3
|
UTSW |
10 |
109,539,233 (GRCm39) |
missense |
probably benign |
0.00 |
R1830:Nav3
|
UTSW |
10 |
109,659,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R1834:Nav3
|
UTSW |
10 |
109,555,883 (GRCm39) |
missense |
probably damaging |
0.99 |
R1881:Nav3
|
UTSW |
10 |
109,688,420 (GRCm39) |
missense |
probably damaging |
0.96 |
R1922:Nav3
|
UTSW |
10 |
109,541,467 (GRCm39) |
missense |
probably benign |
0.43 |
R1944:Nav3
|
UTSW |
10 |
109,552,391 (GRCm39) |
missense |
probably damaging |
0.99 |
R1981:Nav3
|
UTSW |
10 |
109,554,951 (GRCm39) |
splice site |
probably benign |
|
R1985:Nav3
|
UTSW |
10 |
109,606,045 (GRCm39) |
splice site |
probably benign |
|
R1996:Nav3
|
UTSW |
10 |
109,689,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R2051:Nav3
|
UTSW |
10 |
109,660,536 (GRCm39) |
missense |
probably damaging |
0.99 |
R2139:Nav3
|
UTSW |
10 |
109,688,996 (GRCm39) |
missense |
probably benign |
0.22 |
R2248:Nav3
|
UTSW |
10 |
109,532,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R2420:Nav3
|
UTSW |
10 |
109,699,674 (GRCm39) |
missense |
probably damaging |
0.98 |
R2444:Nav3
|
UTSW |
10 |
109,600,776 (GRCm39) |
missense |
probably benign |
0.09 |
R3026:Nav3
|
UTSW |
10 |
109,660,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R3052:Nav3
|
UTSW |
10 |
109,739,613 (GRCm39) |
missense |
probably damaging |
0.99 |
R3441:Nav3
|
UTSW |
10 |
109,540,789 (GRCm39) |
missense |
probably benign |
0.01 |
R3845:Nav3
|
UTSW |
10 |
109,689,237 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3929:Nav3
|
UTSW |
10 |
109,520,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R3932:Nav3
|
UTSW |
10 |
109,529,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R4056:Nav3
|
UTSW |
10 |
109,716,394 (GRCm39) |
critical splice donor site |
probably null |
|
R4057:Nav3
|
UTSW |
10 |
109,716,394 (GRCm39) |
critical splice donor site |
probably null |
|
R4120:Nav3
|
UTSW |
10 |
109,739,605 (GRCm39) |
critical splice donor site |
probably null |
|
R4244:Nav3
|
UTSW |
10 |
109,605,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R4361:Nav3
|
UTSW |
10 |
109,688,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R4512:Nav3
|
UTSW |
10 |
109,529,943 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4514:Nav3
|
UTSW |
10 |
109,529,943 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4700:Nav3
|
UTSW |
10 |
109,600,796 (GRCm39) |
missense |
probably benign |
0.10 |
R4815:Nav3
|
UTSW |
10 |
109,659,413 (GRCm39) |
missense |
probably benign |
|
R4981:Nav3
|
UTSW |
10 |
109,716,553 (GRCm39) |
missense |
probably benign |
|
R5042:Nav3
|
UTSW |
10 |
109,605,129 (GRCm39) |
missense |
probably benign |
0.27 |
R5251:Nav3
|
UTSW |
10 |
109,689,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R5252:Nav3
|
UTSW |
10 |
109,550,152 (GRCm39) |
small deletion |
probably benign |
|
R5273:Nav3
|
UTSW |
10 |
109,528,899 (GRCm39) |
critical splice donor site |
probably null |
|
R5288:Nav3
|
UTSW |
10 |
109,688,966 (GRCm39) |
missense |
probably benign |
0.10 |
R5407:Nav3
|
UTSW |
10 |
109,702,796 (GRCm39) |
missense |
probably benign |
0.28 |
R5533:Nav3
|
UTSW |
10 |
109,719,539 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5561:Nav3
|
UTSW |
10 |
109,552,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R5577:Nav3
|
UTSW |
10 |
109,605,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R5656:Nav3
|
UTSW |
10 |
109,600,494 (GRCm39) |
missense |
probably damaging |
0.96 |
R5872:Nav3
|
UTSW |
10 |
109,600,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R6023:Nav3
|
UTSW |
10 |
109,659,376 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6061:Nav3
|
UTSW |
10 |
109,702,845 (GRCm39) |
nonsense |
probably null |
|
R6189:Nav3
|
UTSW |
10 |
109,555,880 (GRCm39) |
missense |
probably damaging |
0.98 |
R6214:Nav3
|
UTSW |
10 |
109,688,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6215:Nav3
|
UTSW |
10 |
109,688,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6264:Nav3
|
UTSW |
10 |
109,524,694 (GRCm39) |
missense |
probably damaging |
0.97 |
R6500:Nav3
|
UTSW |
10 |
109,600,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Nav3
|
UTSW |
10 |
109,555,891 (GRCm39) |
missense |
probably damaging |
0.99 |
R6868:Nav3
|
UTSW |
10 |
109,529,027 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7079:Nav3
|
UTSW |
10 |
109,603,153 (GRCm39) |
missense |
probably benign |
0.16 |
R7099:Nav3
|
UTSW |
10 |
109,539,195 (GRCm39) |
missense |
probably benign |
0.11 |
R7139:Nav3
|
UTSW |
10 |
109,689,338 (GRCm39) |
missense |
probably benign |
0.44 |
R7238:Nav3
|
UTSW |
10 |
109,689,185 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7338:Nav3
|
UTSW |
10 |
109,605,073 (GRCm39) |
missense |
probably benign |
0.04 |
R7343:Nav3
|
UTSW |
10 |
109,739,619 (GRCm39) |
missense |
probably damaging |
0.98 |
R7383:Nav3
|
UTSW |
10 |
109,552,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R7391:Nav3
|
UTSW |
10 |
109,539,317 (GRCm39) |
missense |
probably benign |
0.07 |
R7399:Nav3
|
UTSW |
10 |
109,688,795 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7457:Nav3
|
UTSW |
10 |
109,532,189 (GRCm39) |
nonsense |
probably null |
|
R7462:Nav3
|
UTSW |
10 |
109,659,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R7542:Nav3
|
UTSW |
10 |
109,659,394 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7659:Nav3
|
UTSW |
10 |
109,602,851 (GRCm39) |
missense |
probably benign |
0.09 |
R7749:Nav3
|
UTSW |
10 |
109,539,213 (GRCm39) |
missense |
probably damaging |
0.99 |
R7794:Nav3
|
UTSW |
10 |
109,524,717 (GRCm39) |
missense |
probably benign |
0.08 |
R7876:Nav3
|
UTSW |
10 |
109,689,359 (GRCm39) |
missense |
probably benign |
0.26 |
R8048:Nav3
|
UTSW |
10 |
109,600,779 (GRCm39) |
missense |
probably benign |
0.13 |
R8104:Nav3
|
UTSW |
10 |
109,594,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R8125:Nav3
|
UTSW |
10 |
109,688,520 (GRCm39) |
missense |
probably damaging |
0.99 |
R8275:Nav3
|
UTSW |
10 |
109,527,984 (GRCm39) |
missense |
noncoding transcript |
|
R8325:Nav3
|
UTSW |
10 |
109,541,464 (GRCm39) |
missense |
probably benign |
0.24 |
R8336:Nav3
|
UTSW |
10 |
109,603,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R8523:Nav3
|
UTSW |
10 |
109,659,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R8529:Nav3
|
UTSW |
10 |
109,689,192 (GRCm39) |
missense |
probably benign |
0.09 |
R8745:Nav3
|
UTSW |
10 |
109,659,311 (GRCm39) |
missense |
probably benign |
0.08 |
R8752:Nav3
|
UTSW |
10 |
109,596,165 (GRCm39) |
intron |
probably benign |
|
R8794:Nav3
|
UTSW |
10 |
109,605,032 (GRCm39) |
nonsense |
probably null |
|
R8816:Nav3
|
UTSW |
10 |
109,699,721 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9029:Nav3
|
UTSW |
10 |
109,699,613 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9117:Nav3
|
UTSW |
10 |
109,520,100 (GRCm39) |
missense |
probably benign |
0.41 |
R9126:Nav3
|
UTSW |
10 |
109,541,524 (GRCm39) |
missense |
probably benign |
|
R9258:Nav3
|
UTSW |
10 |
109,550,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R9347:Nav3
|
UTSW |
10 |
109,738,955 (GRCm39) |
missense |
probably damaging |
0.98 |
R9353:Nav3
|
UTSW |
10 |
109,554,065 (GRCm39) |
missense |
probably damaging |
0.99 |
R9366:Nav3
|
UTSW |
10 |
109,659,364 (GRCm39) |
missense |
probably damaging |
0.99 |
R9384:Nav3
|
UTSW |
10 |
109,554,158 (GRCm39) |
missense |
probably damaging |
0.98 |
R9428:Nav3
|
UTSW |
10 |
109,605,176 (GRCm39) |
missense |
probably benign |
|
R9454:Nav3
|
UTSW |
10 |
109,835,864 (GRCm39) |
missense |
probably benign |
0.01 |
R9516:Nav3
|
UTSW |
10 |
109,520,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R9521:Nav3
|
UTSW |
10 |
109,835,845 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9622:Nav3
|
UTSW |
10 |
109,603,103 (GRCm39) |
missense |
probably benign |
|
R9689:Nav3
|
UTSW |
10 |
109,605,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R9796:Nav3
|
UTSW |
10 |
109,527,969 (GRCm39) |
missense |
probably damaging |
0.99 |
X0012:Nav3
|
UTSW |
10 |
109,527,958 (GRCm39) |
missense |
probably damaging |
1.00 |
|